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The in vivo Gene Editing and Critical Components Process Development team in the Technical Development Department is seeking a highly motivated Process Engineer for the process and formulation development of critical gene editing components and drug products [e.g. Ribonucleoprotein (RNP), messenger RNA (mRNA) & Lipid Nanoparticle (LNP.
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Lead internal process development, optimization and tech transfer of upstream and downstream process development for clinical development pipeline. Seasoned leader with extensive industry experince in biologic CMC and process development at the VP level.
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The successful candidate will understand financial drivers of the HomeStart business, will focus on finance/accounting process improvement and will be a hands-on operational manager who is both comfortable with details as well as able to lead the financial strategy of HomeStart.
$130,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Perform structural repair, alterations, or improvement work such as preparing surfaces for plaster or cement work; studding, wiring, and plastering walls. Job Competencies: All applicants must be able, through the interview process, to demonstrate knowledge and understanding of the following areas.
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Conduct regular process audits and reviews to identify areas for improvement and implement best practices. This position requires a deep understanding of pharmaceutical manufacturing principles, process engineering, and regulatory compliance.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS, RTU), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client's facility.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Dual certification or Certified Documentation Improvement Practitioner (CDIP)/Certified Clinical Documentation Specialist (CCDS) credentials are highly preferred. Dual certification or Certified Documentation Improvement Practitioner (CDIP)/Certified Clinical Documentation Specialist (CCDS) credentials are highly preferred.
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Cerevel Therapeutics is seeking a talented synthetic organic chemist for a role in Process Development as a Principal Scientist. The Principal Scientist will apply and grow their expertise in small molecule drug substance synthetic process development as they contribute to Cerevel’s pursuit of its rich small molecule pipeline spanning pre-clinical through commercial candidates.
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You will support hardware and software development teams, Reliability Engineering, Systems Engineering, and GNC. The right person for this role has knowledge of design, development, test, analysis, manufacturing, operations, asset tracking and maintenance, and continuous improvement.
$120,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Communicating all process inefficiencies, equipment malfunctions, safety concerns and GMP issues to the Production Supervisor & Sanitation Supervisor. The Maintenance Supervisor will interface with Production Supervisors, leads, and operators to gather information on issues surrounding the performance of Production and Process equipment.
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Atrius Health, a pioneer and leader of value-based care in the country, is nationally recognized for transforming healthcare through clinical innovations and quality improvement. Atrius Health, a pioneer and leader of value-based care in the country, is nationally recognized for transforming healthcare through clinical innovations and quality improvement.
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Drive continuous improvement and innovation in product formulations, staying on top of new technologies and scientific advancements in the cosmetic industry. Bachelor’s or master’s degree in Chemistry, Chemical Engineering, Cosmetic Science, or a related field.
$125,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience with project work and process knowledge of hydrology and hydraulics, grading and drainage, streets, bridges, pump and system-curve analysis, dam experience, and other structures, preferred.
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The Radiologic Technologist/Mammographer will also take part in Quality Improvement and Quality Control activities. The Radiologic Technologist/Mammographer is expected to produce high quality Radiographic and mammographic images under the guidance of the Radiology Supervisor.
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Principal Scientist, Protein Production and Process Development. and with proteins expressed in mammalian cells with oversight of both upstream and downstream process development. We are seeking an experienced Protein Production and Process Development leader with experience producing protein lead and Development Candidate molecules, preferably with both mammalian and.
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process improvement jobs Company: Ekidzcare in Boston, MA
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